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首页> 外文期刊>The Journal of Comparative Neurology >Distribution of TAG-1 and synaptophysin in the developing cerebellar cortex: relationship to Purkinje cell dendritic development.
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Distribution of TAG-1 and synaptophysin in the developing cerebellar cortex: relationship to Purkinje cell dendritic development.

机译:TAG-1和突触素在小脑皮质发育中的分布:与浦肯野细胞树突状发育的关系。

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During postnatal cerebellar development, differentiating Purkinje cell (PC) dendrites extend towards the pial surface and progressively contact immature granule cell parallel fiber (PF) axons in the deep external granule layer (EGL), thus forming a zone of synaptic contact called the molecular layer (ML). The neuronal cell adhesion molecule, TAG-1, is transiently expressed on PF axons in the deep EGL (Yamamoto et al. [1986] J. Neurosci. 12:3576-3594). To determine the spatiotemporal relationship between Purkinje cell dendritic differentiation and the cessation of TAG-1 expression, sagittal sections from developing rat cerebellum were double-labeled for TAG-1 and the Purkinje cell-specific marker, calbindin, by using indirect immunofluorescence. At postnatal day 2 (P2) and P5, confocal microscopy revealed that TAG-1 immunoreactivity began above the furthest superficial extent of the Purkinje cell apical dendritic cap. By P10, PC dendrites penetrated partially into the TAG-1-positive deep EGL, creating a narrow region of overlap in TAG-1/calbindin staining at the deep EGL/ML border. In contrast, at P15 and P20, TAG-1 staining began directly above the furthest superficial extent of the Purkinje cell dendrites, with little or no overlap in TAG-1/calbindin staining. Staining for the synaptic vesicle glycoprotein, synaptophysin, was dim throughout most of the TAG-1-positive deep EGL, although bright synaptophysin immunoreactivity was observed throughout the ML. Overlap in TAG-1/synaptophysin staining was observed primarily at the deep EGL/ML border, suggesting that robust expression of synaptophysin in granule cells does not begin until after contact with Purkinje cell dendrites has been initiated. Our results suggest that factors present in the developing ML may influence the cessation of TAG-1 expression and the initiation of synaptophysin expression at the border region between the ML and the deep EGL.
机译:在产后小脑发育过程中,分化的浦肯野细胞(PC)树突向着皮膜表面延伸,并逐渐接触未成熟的颗粒细胞平行纤维(PF)轴突在深部外部颗粒层(EGL)中,从而形成称为分子层的突触接触区。 (ML)。神经细胞粘附分子TAG-1在深层EGL中的PF轴突上瞬时表达(Yamamoto等人,[1986] J.Neurosci.12:3576-3594)。为了确定Purkinje细胞树突分化与TAG-1表达停止之间的时空关系,使用间接免疫荧光技术将来自发育中大鼠小脑的矢状切面双标记TAG-1和Purkinje细胞特异性标志物calbindin。在产后第2天(P2)和P5,共聚焦显微镜检查显示TAG-1免疫反应性开始于Purkinje细胞根尖树突状帽的最浅表层上方。通过P10,PC树突部分渗透到TAG-1阳性深层EGL中,从而在EGL / ML深层边界处的TAG-1 / calbindin染色中形成了一个狭窄的重叠区域。相反,在P15和P20处,TAG-1染色直接开始于Purkinje细胞树突最表面的上方,而TAG-1 / calbindin染色几乎没有重叠。尽管在整个ML中观察到明亮的突触素免疫反应性,但在大多数TAG-1阳性深层EGL中,突触囊泡糖蛋白突触素的染色较暗。 TAG-1 /突触素染色的重叠主要在深EGL / ML边界处观察到,表明突触素在颗粒细胞中的稳健表达直到与Purkinje细胞树突接触后才开始。我们的结果表明,存在于正在发展的ML中的因素可能影响TAG-1表达的停止和ML与深层EGL之间边界区域突触素表达的启动。

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